Shockwave intravascular lithotripsy system: medical device reports filed with FDA

459 reports carry this product code, 2021–2026; 0 brands with a page.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "Although MDRs are a valuable source of information, this passive surveillance system has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data. In addition, the incidence or prevalence of an event cannot be determined from this reporting system alone due to potential under-reporting of events and lack of information about frequency of device use." And: "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices."

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

459
reports with this product code: 0% of all MAUDE reports; 121
reports, 12 months to August 2026: 116 in the 12 months before; 20.5%
classified as malfunction: 62.3% across all reports; 21.8%
classified as death, as reported: 0.9% across all reports

Product code QMG is FDA's classification for "Shockwave intravascular lithotripsy system" (unknown panel), a class 3 device. 459 medical device reports carry this product code, 0% of the MAUDE database, from May 2021 to August 2026.

121 reports arrived in the 12 months to August 2026, close to the 116 of the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are injury (57.3%), death (21.8%) and malfunction (20.5%). 0 brand names with a page on this site carry this code; the brands table is ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Brands with this product code

Brand	Reports	Latest 12 months	Classified as death	Classified as malfunction

Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Reports by month, five years

FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.

Event type and report source

Event type

Death21.8%100

Injury57.3%263

Malfunction20.5%94

Other0.2%1

Not given0.2%1

Who filed

Manufacturer report85.8%394

Voluntary report3.5%16

User facility report0%0

Distributor report0%0

Not given10.7%49

Grey bar: all 26,136,888 MAUDE reports.

Device problems coded

Device problem (FDA code)	Reports	Share
Material split, cut or torn	59	12.9%
Detachment of device or device componentpart of the device came off	33	7.2%
Difficult to removethe device was hard to remove	33	7.2%
Difficult to advance	25	5.4%
Material rupture	24	5.2%
Off-label use	16	3.5%
Insufficient device problem information	15	3.3%
Breakthe device broke	9	2%
Entrapment of device	8	1.7%
Failure to cycle	7	1.5%
Failure to deflate	7	1.5%
Deformation due to compressive stress	6	1.3%
Material separation	6	1.3%
Deflation problem	5	1.1%
Inflation problem	4	0.9%
Sparking	4	0.9%
Activation failure	2	0.4%
Difficult or delayed positioning	2	0.4%
Material puncture/hole	2	0.4%
Partial blockage	2	0.4%

Questions about shockwave intravascular lithotripsy system reports

What is product code QMG?

FDA's classification code for "Shockwave intravascular lithotripsy system", class 3, reviewed by the unknown panel. Every device report carries the product code of the device involved.

How many reports carry this code?

459 reports through August 2026, 121 of them in the latest 12 months.

Which brands appear most often?

No brand with a page on this site.

Can the brands table be used to rank the devices?

No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." Brands differ in how many are in use, how long they have been sold and how reports are collected.

Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.

Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.